2-(2,2-Difluoroethoxy)bromobenzene
Artikel-Nr:
(BOSSBS-11363R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11363R-FITC
Lokale Artikelnummer::
BOSSBS-11363R-FITC
Beschreibung:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9261R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9261R-FITC
Lokale Artikelnummer::
BOSSBS-9261R-FITC
Beschreibung:
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF185 (ring finger protein 185), also known as FLJ38628, is a 192 amino acid multi-pass membrane protein containing one RING-type zinc finger. Two RNF185 isoforms exist as a result of alternative splicing, and the gene encoding RNF185 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11363R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11363R-A647
Lokale Artikelnummer::
BOSSBS-11363R-A647
Beschreibung:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Digalliumtrisulfid ≥99,999% (Metall-Basis)
Lieferant:
Alfa Aesar
Beschreibung:
4,5-Dichlor-3(2H)-pyridazinon ≥98%
Lieferant:
Alfa Aesar
Beschreibung:
1,8-Diazabicyclo[5.4.0]-7-undecen ≥99%
Artikel-Nr:
(BOSSBS-1724R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1724R
Lokale Artikelnummer::
BOSSBS-1724R
Beschreibung:
Motilin is a 22 amino acid peptide hormone expressed throughout the gastrointestinal (GI) tract. The protein encoded by this gene is a motilin receptor which is a member of the G-protein coupled receptor 1 family. This member is a multi-pass transmembrane protein, and is an important therapeutic target for the treatment of hypomotility disorders.
VE:
1 * 100 µl
Artikel-Nr:
(91124.001)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC91124.001
Beschreibung:
A standard mixture, typically used for food testing, containing the following components: 100 ug/ml each of Alanycarb [CAS:83130-01-2] ; Aldicarb [CAS:116-06-3] ; Aldicarb-sulfone [CAS:1646-88-4] ; Aldicarb-sulfoxide [CAS:1646-87-3] ; Benfuracarb [CAS:82560-54-1] ; Butocarboxim [CAS:34681-10-2] ; Butocarboxim-sulfone [CAS:34681-23-7] ; Ethiofencarb [CAS:29973-13-5] ; Furathiocarb [CAS:65907-30-4] ; Methabenzthiazuron [CAS:18691-97-9] ; Methiocarb [CAS:2032-65-7] ; Methomyl [CAS:16752-77-5] ; Oxamyl [CAS:23135-22-0] ; Tebuthiuron [CAS:34014-18-1] ; Thidiazuron [CAS:51707-55-2] ; Thiophanate-methyl [CAS:23564-05-8] in Acetonitrile
VE:
1 * 1 mL
Artikel-Nr:
(BLDPBD20227-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD20227-250MG
Lokale Artikelnummer::
BLDPBD20227-250MG
Beschreibung:
9,9-Dimethylfluorene-2,7-diboronic acid bis(pinacol) ester 97%
VE:
1 * 250 mg
Artikel-Nr:
(ROCK600-403-466)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
600-403-466
Lokale Artikelnummer::
ROCK600-403-466
Beschreibung:
Anti-KLH Antibody Peroxidase Conjugated antibody has been assayed against 1.0 µg of KLH in a standard capture ELISA using ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) substrate for 30 minutes at room temperature.
VE:
1 * 100 µG
Artikel-Nr:
(BLDPBD129758-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD129758-500G
Lokale Artikelnummer::
BLDPBD129758-500G
Beschreibung:
EDTA Trikaliumsalz 98+%
VE:
1 * 500 g
Artikel-Nr:
(ROCK601-4602)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
601-4602
Lokale Artikelnummer::
ROCK601-4602
Beschreibung:
Anti-Bovine IgG (H&L) has been assayed against 1.0 µg of Bovine IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) as a substrate for 30 minutes at room temperature.
VE:
1 * 2 mg
Artikel-Nr:
(ROCK616-1602)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
616-1602
Lokale Artikelnummer::
ROCK616-1602
Beschreibung:
Anti-Donkey IgG (H&L) has been assayed against 1.0 µg of Donkey IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) as a substrate for 30 minutes at room temperature.
VE:
1 * 2 mg
Artikel-Nr:
(BOSSBS-11722R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11722R-A680
Lokale Artikelnummer::
BOSSBS-11722R-A680
Beschreibung:
Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin 1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterised by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11722R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11722R-A350
Lokale Artikelnummer::
BOSSBS-11722R-A350
Beschreibung:
Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin ?1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterized by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt抯 lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
VE:
1 * 100 µl
Artikel-Nr:
(ACRO412250250)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
412250250
Lokale Artikelnummer::
ACRO412250250
Beschreibung:
Imidazol-4,5-dicarbonsäure 99%
VE:
1 * 25 g
Preis auf Anfrage
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